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MK0991, caspofungin · 3 trials · 3 indications
| Name | Type | Description |
|---|---|---|
| MK0991, caspofungin acetate / Duration of Treatment: | DRUG | - |
| MK0991, caspofungin acetate/Duration of Treatment: variable | DRUG | - |
| MK0991, caspofungin acetate | DRUG | - |
| Comparator: amphotericin B | DRUG | - |
| Comparator: lipid formulation of amphotericin B and/or azole | DRUG | - |
Inclusion Criteria: * Patient has had an absolute neutrophil count \< 500/mm3 for at least 96 hours (the patient must not be expected to recover from neutropenia in the next 48 hours), and has received at least 96 hours of parenteral broad spectrum systemic antibacterial therapy preceding study ent...
Top 1 of 6 competitors
| Company | Ticker | Trials | Lead Phase | Drugs |
|---|---|---|---|---|
| Merck & Co., Inc. | MRK | 1 | PHASE2 | Posaconazole |
MK0991 is an investigational small molecule being studied for the treatment of aspergillosis, a fungal infection. It is currently in Phase 2 clinical development and has been evaluated in combination with standard antifungal agents for salvage therapy of invasive aspergillosis.
MK0991 is being developed by Merck & Company, Inc., which trades on the New York Stock Exchange under the ticker symbol MRK. The company is conducting clinical trials to evaluate the drug's safety and efficacy in patients with aspergillosis.
MK0991 is in Phase 2 clinical development for aspergillosis. It is an investigational drug, meaning it has not yet been approved by regulatory authorities and is still undergoing clinical evaluation to determine its safety and effectiveness.
MK0991 has been studied in a completed Phase 2 clinical trial with the identifier NCT00076869. This trial evaluated MK0991 in combination with standard antifungal agents for the treatment of salvage invasive aspergillosis and enrolled 55 participants aged 16 years and older.
Yes, MK0991 is also known as caspofungin. Both names refer to the same investigational drug being developed by Merck & Company, Inc. for the treatment of aspergillosis. The drug is currently in Phase 2 clinical trials.